FDA.reportPublic FDA data

Furosemide

Product NDC
43063-849
11-digit product format
430630849
Labeler code
43063
Product ID
43063-849_39fd20b5-22d0-8252-e063-6294a90adaad
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA076796
Marketing category
ANDA
Marketing start
2004-03-26
Substance
FUROSEMIDE
Active strength
20 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Furosemide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FUROSEMIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7LXU5N7ZO5
Rxcui310429

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d80d3aff-3a63-4d7b-a2be-fd9388b04330Product name920250806
9061e89f-9c86-4196-b34b-886fc1673cc4Product name120140821

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43063-849-21Furosemide21 in 1 BOTTLE, PLASTICTABLET2117
43063-849-30Furosemide30 in 1 BOTTLE, PLASTICTABLET3017
43063-849-60Furosemide60 in 1 BOTTLE, PLASTICTABLET6017
43063-849-90Furosemide90 in 1 BOTTLE, PLASTICTABLET9017

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-849-21EA - Each43063-8498da46905-358f-45ac-98b0-8267c268ef8e12018-06-11
43063-849-30EA - Each43063-84904a3bb53-9808-4c3d-8b3f-4c5b538a40a912018-06-11
43063-849-60EA - Each43063-849527258d4-e65e-413a-9022-fd9c482104ff12018-06-11
43063-849-90EA - Each43063-849ec3a494c-dbe9-4132-8235-0cde3ae171db12018-06-11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43063-849FUROSEMIDE TABLET [PD-RX PHARMACEUTICALS, INC.]15Current NDC, Legacy NDC, 4 package rows20241017_3ba730ab-90d4-478a-80b3-1ea3edb03e4d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN3ba730ab-90d4-478a-80b3-1ea3edb03e4d17
310429furosemide 20 MG Oral TabletSCD3ba730ab-90d4-478a-80b3-1ea3edb03e4d17

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43063-849-214306308492121 TABLET in 1 BOTTLE, PLASTIC (43063-849-21) 21 tablet2018-04-270000-00-00NoNoCurrent
43063-849-304306308493030 TABLET in 1 BOTTLE, PLASTIC (43063-849-30) 30 tablet2018-04-270000-00-00NoNoCurrent
43063-849-604306308496060 TABLET in 1 BOTTLE, PLASTIC (43063-849-60) 60 tablet2018-05-030000-00-00NoNoCurrent
43063-849-904306308499090 TABLET in 1 BOTTLE, PLASTIC (43063-849-90) 90 tablet2018-05-030000-00-00NoNoCurrent